Imaging Endpoints, a global leader in imaging clinical research and oncology trials, is hiring a Clinical Project Coordinator (CPC / CPC II) for its Hyderabad office. This opportunity is ideal for life science, pharmacy, and clinical research professionals seeking a career in imaging-based clinical trials without direct patient interaction.
Imaging Endpoints (IE) is the world’s largest Imaging Clinical Research Organization (iCRO), supporting multiple global oncology drug approvals and working with leading sponsors across the US, Europe, and Asia.
About Imaging Endpoints
Imaging Endpoints is passionately focused on its mission: “Connect Imaging to the Cure™.”
Headquartered in Scottsdale, Arizona, with global offices including Hyderabad, India, IE collaborates with sponsors, CROs, and sites to optimize imaging endpoints in clinical trials—especially in oncology research.
Job Details
- Job Title: Clinical Project Coordinator / Clinical Project Coordinator II
- Company: Imaging Endpoints
- Location: Hyderabad, Telangana
- Employment Type: Full-time, On-site
- Experience Level: Fresher to 2+ years (role-dependent)
- Industry: Imaging CRO / Clinical Research / Oncology Trials
Key Responsibilities – Clinical Project Coordinator
- Conduct site evaluations to assess imaging capability per SOPs
- Act as primary point of contact for clinical trial sites
- Coordinate and schedule site trainings
- Maintain and own the Trial Master File (TMF)
- Ensure audit readiness and support internal/external audits
- Verify study and read start-up activities in coordination with Project Managers
- Track study enrollment and maintain project trackers
- Perform User Acceptance Testing (UAT) when assigned
- Track imaging data received via CD or SFTP and upload to PACS repositories (AG Mednet)
- Support CTIS and DTF preprocessing activities
- Manage CRFs, queries, and clinical data flow
- Convert clinical dossiers for reader assignments
- Prepare and share weekly status, site, and enrollment reports
- Schedule meetings, prepare agendas, and document minutes
- Ensure compliance with GCP, regulatory guidelines, and HIPAA
Additional Responsibilities – Clinical Project Coordinator II
- Collaborate with PMs on site lists, system access (CTMS, AG Mednet)
- Mentor and train junior CPCs
- Lead study close-out activities and timeline alignment
- Perform image reconciliation
- Ensure end-to-end compliance throughout the project lifecycle
Qualifications & Eligibility
🎓 Education
- Bachelor’s degree required
(B.Pharm, M.Pharm, B.Sc / M.Sc Life Sciences, Biotechnology, Clinical Research, or related fields preferred)
💼 Experience
- 0–1 year (CPC) | 1+ year (CPC II) in clinical trials / healthcare / imaging / CRO
- Prior experience as a Clinical Research Coordinator (CRC) is an advantage
📘 Knowledge & Skills
- Understanding of GCP, QA/Compliance, TMF management
- Proficiency in MS Office & internet applications
- Strong communication, documentation, and organizational skills
- Ability to manage multiple priorities under tight timelines
- High attention to detail and confidentiality
Why Join Imaging Endpoints?
- Work with the world’s leading oncology iCRO
- Exposure to global clinical trials and advanced imaging technology
- Strong learning, mentoring, and career growth environment
- High ethical standards and patient-centric mission
- Collaborative global teams across the US, Europe, and Asia